journal article·2019-10-28

Abundant Organic Dye as an Anolyte for Aqueous Flow Battery with Multielectron Transfer

Alolika Mukhopadhyay, Huijuan Zhao, Bin Li, Jonathan Hamel, Yang Yang, Daxian Cao, Avi Natan, Hongli Zhu

ACS Applied Energy Materials· Volume 2· Issue 10
Publisher page

Abstract

Organic redox flow batteries have the potential to surpass the challenges posed by inorganic electrolytes commonly used in flow batteries, thus achieving high performance and a sophisticated storage solution for the grid. Herein, we demonstrated a high performance aqueous organic redox flow battery (AORFB) utilizing a redox-active resource from nature, indigo carmine (5,5′-indigodisulfonic acid sodium salt) (IC-Na), as the anolyte. The 5,5′-indigodisulfonic acid (IC-H) is obtained through the substitution of sodium ions in IC-Na with protons (H+). The aqueous solubility of IC-H was increased dramatically from 0.035 to 0.760 M (1.52 M electron concentration) in protic solvents. The diffusion coefficients (IC-Na, 1.06 × 10–5 cm2 s –1; IC-H, 2.19 × 10–5 cm2 s –1) and reaction rate constants (IC-Na, 1.93 × 10–4 cm s –1; IC-H, 1.86 × 10–4 cm s–1) of IC-Na and IC-H indicate rapid reaction kinetics. The highly soluble and affordable IC-H with fast redox kinetics was used as a sustainable anolyte by pairing with different catholytes. Moreover, a computational study was conducted which signifies the prospect of further improvements in solubility and voltage window by tuning the structure. Therefore, the environmentally benign and earth-abundant IC-H represents a promising choice for green and sustainable redox active anolyte of AORFB.
Source: openalex_inverted_index · Quality: baseline

Research context

OpenAlex topics: Advanced battery technologies research · Electrocatalysts for Energy Conversion · Advanced Battery Technologies Research

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Mechanical and Industrial Engineering, Northeastern University, 360 Huntington Avenue, Boston, Massachusetts 02115, United States

Mechanical Engineering Department, Clemson University, 201 Fluor Daniel EIB, Clemson, South Carolina 29634-0921, United States

Electrochemical Materials and System Group, Pacific Northwest National Laboratory, 902 Battelle Boulevard, Richland, Washington 99352, United States

Funding

Northeastern University

References (49)

Show source-provided references
1. 10.1021/acsenergylett.7b0065010.1021/acsenergylett.7b00650 ↗
2. 10.1038/nenergy.2016.10210.1038/nenergy.2016.102 ↗
3. 10.1149/2.0741712jes10.1149/2.0741712jes ↗
4. 10.1021/acsenergylett.7b0001910.1021/acsenergylett.7b00019 ↗
5. 10.1021/acssuschemeng.8b0022110.1021/acssuschemeng.8b00221 ↗
6. 10.1002/aenm.20160148810.1002/aenm.201601488 ↗
7. 10.1126/science.aab303310.1126/science.aab3033 ↗
8. 10.1039/c2cc32466k10.1039/c2cc32466k ↗
9. 10.1149/2.1371607jes10.1149/2.1371607jes ↗
10. 10.1002/aenm.20150144910.1002/aenm.201501449 ↗
11. 10.1002/adma.20140374610.1002/adma.201403746 ↗
12. 10.1002/ange.20171051710.1002/ange.201710517 ↗
13. 10.1038/natrevmats.2016.8010.1038/natrevmats.2016.80 ↗
14. 10.1002/aenm.20160148810.1002/aenm.201601488 ↗
15. 10.1038/nature1290910.1038/nature12909 ↗
16. 10.1021/acssuschemeng.8b0022110.1021/acssuschemeng.8b00221 ↗
17. 10.1038/s41560-018-0167-310.1038/s41560-018-0167-3 ↗
18. 10.1039/C7TA06573F10.1039/C7TA06573F ↗
19. 10.1016/j.joule.2018.10.01010.1016/j.joule.2018.10.010 ↗
20. 10.1016/j.nanoen.2017.10.05710.1016/j.nanoen.2017.10.057 ↗
21. 10.1038/nature1574610.1038/nature15746 ↗
22. 10.1039/C6EE01883A10.1039/C6EE01883A ↗
23. 10.1016/j.jclepro.2009.05.00710.1016/j.jclepro.2009.05.007 ↗
24. 10.1016/j.ssnmr.2015.08.00410.1016/j.ssnmr.2015.08.004 ↗
25. König J. · 2015 · 3510.1016/B978-1-78242-011-8.00002-7 ↗
26. Harp B. P. · 2015 · 7510.1016/B978-1-78242-011-8.00004-0 ↗
27. 10.1039/b209630g10.1039/b209630g ↗
28. 10.1039/b403601h10.1039/b403601h ↗
29. 10.1002/adma.20060037510.1002/adma.200600375 ↗
30. 10.1179/2047058412Y.000000005810.1179/2047058412Y.0000000058 ↗
31. 10.1177/004051750934231910.1177/0040517509342319 ↗
32. Barden T. C. · 2010 · 3110.1007/7081_2010_48 ↗
33. 10.1002/elan.20130015510.1002/elan.201300155 ↗
34. 10.1039/c3cp52763h10.1039/c3cp52763h ↗
35. 10.1080/08927022.2011.57813610.1080/08927022.2011.578136 ↗
36. 10.1016/j.ijhydene.2017.07.04910.1016/j.ijhydene.2017.07.049 ↗
37. 10.1002/aenm.20170205610.1002/aenm.201702056 ↗
38. 10.1002/aenm.20150144910.1002/aenm.201501449 ↗
39. 10.1021/jacs.7b0014710.1021/jacs.7b00147 ↗
40. 10.1016/j.jphotochem.2010.04.00210.1016/j.jphotochem.2010.04.002 ↗
41. 10.1016/j.ijhydene.2016.12.06310.1016/j.ijhydene.2016.12.063 ↗
42. 10.1007/s10800-016-1033-210.1007/s10800-016-1033-2 ↗
43. 10.1021/acsenergylett.7b0130210.1021/acsenergylett.7b01302 ↗
44. 10.1021/jacs.6b1098410.1021/jacs.6b10984 ↗
45. 10.1002/anie.20171051710.1002/anie.201710517 ↗
46. Haynes W. M. · 2015
47. 10.1039/C6MH00016A10.1039/C6MH00016A ↗
48. 10.1002/adfm.20190319210.1002/adfm.201903192 ↗
49. 10.1063/1.44707910.1063/1.447079 ↗